Ramco Laboratories, Inc.
FDA 510(k) & PMA Approved Devices — 9 products
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Total Devices9
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K983107 | VFE | GGP | 1998-10-22 | View |
| 510(k) | K981208 | TFR | JNM | 1998-10-21 | View |
| 510(k) | K910481 | EPO-RIA | GGT | 1991-11-29 | View |
| 510(k) | K872941 | SPECTRO C | GGP | 1987-09-04 | View |
| 510(k) | K864701 | VWF IMMUNOBLOT | GGP | 1987-03-30 | View |
| 510(k) | K861159 | SPECTRO VWF | GGP | 1986-05-01 | View |
| 510(k) | K831470 | PTH MR | CEW | 1983-06-22 | View |
| 510(k) | K823016 | CANDIDA DETECTION SYSTEM | LHK | 1982-12-28 | View |
| 510(k) | K812056 | SPECTRO FEIRITIN | DBF | 1981-08-12 | View |
No matching devices.
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